Canonical Allele Identifier: CA345497342

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027272G>A (hg19) ; chr1:g.244863970G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863970G>A , CM000663.2:g.244863970G>A	GRCh38
NC_000001.10:g.245027272G>A , CM000663.1:g.245027272G>A	GRCh37
NC_000001.9:g.243093895G>A	NCBI36
NG_042184.1:g.5556C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000704074.1:c.16C>T
ENST00000283179.14:c.338C>T	ENSP00000283179.10:p.Ala113Val
ENST00000444376.7:c.338C>T	ENSP00000393151.2:p.Ala113Val
ENST00000476241.2:n.523C>T
ENST00000638475.1:c.122C>T	ENSP00000491305.1:p.Ala41Val
ENST00000638952.1:n.569C>T
ENST00000640218.2:c.338C>T MANE Select	ENSP00000491215.1:p.Ala113Val
ENST00000640306.1:c.338C>T	ENSP00000491685.1:p.Ala113Val
ENST00000640440.1:c.38C>T	ENSP00000491263.1:p.Ala13Val
ENST00000649899.1:n.562C>T
ENST00000283179.13:c.338C>T	ENSP00000283179.9:p.Ala113Val
ENST00000444376.6:c.338C>T	ENSP00000393151.2:p.Ala113Val
ENST00000476241.1:n.522C>T
NM_004501.3:c.338C>T	NP_004492.2:p.Ala113Val
NM_031844.2:c.338C>T	NP_114032.2:p.Ala113Val
NM_031844.3:c.338C>T MANE Select	NP_114032.2:p.Ala113Val